The DOI matches its Crossref record; 31 of the 32 references it cites were found in a registry or an index.
Dendritic cell–derived hepcidin sequesters iron from the microbiota to promote mucosal healing
Open accessAbstract
Ironing out the details of mucosal healing: Anemia is a frequent complication of disorders such as inflammatory bowel disease, occurring in part as a result of increased bleeding into the intestine. Bessman et al. show that the peptide hormone hepcidin, which regulates systemic iron homeostasis, is required for intestinal repair in a mouse model of inflammatory bowel disease (see the Perspective by Rescigno). This effect was independent of hepatocyte-produced hepcidin and systemic iron levels. Instead, production of hepcidin by conventional dendritic cells was necessary and sufficient to promote local iron sequestration by macrophages, which in turn modulated the makeup of the gut microbiota to one with a more beneficial distribution of species. Science , this issue p. 186 ; see also p. 129
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
The cited source says what the claim attributes to it.
In the citing paper
“Absence of local hepcidin production or insensitivity of macrophage ferroportin to hepcidin is thought to result in higher local extracellular iron concentrations, affecting the growth of luminal and tissue-infiltrating bacteria and worsening DSS-induced colitis.”
From Hepcidin-Ferroportin Interaction Controls Systemic Iron Homeostasis (2021) · cites this paper as [49]
The cited source says what the claim attributes to it.
In the citing paper
“In a mouse model of colitis, the hepcidin-ferroportin interaction in the intestine was shown to be important for mucosal healing [49].”
From Hepcidin-Ferroportin Interaction Controls Systemic Iron Homeostasis (2021) · cites this paper as [49]
In the citing paper
“Within favorable taxa, we identified increased abundance of genes related to polysaccharide deacetylation known to play a role in immune evasion42, as well as iron transport and iron-induced production of reactive oxygen species ROS, which affect mucosal healing43.”
From Intestinal microbiota signatures of clinical response and immune-related adverse events in melanoma patients treated with anti-PD-1 (2022) · cites this paper as [43]
In the citing paper
“Recently, in an experimental murine dextran sodium sulphate‐driven colitis, HAMP production by dendritic cells was proposed to drive local iron sequestration in colonic myeloid cells, limiting increases in free iron driven by loss of barrier integrity and tissue damage.”
From The battle for iron in enteric infections (2020) · cites this paper as [107]
In the citing paper
“Failure to sequester iron locally resulted in dysbiosis, increased microbial translocation across the mucosa, persistent gut inflammation and failure to recover weight 107 (Fig. 2).”
From The battle for iron in enteric infections (2020) · cites this paper as [107]
In the citing paper
“Conversely, iron‐deficient diets in experimental systems seem to favour the growth of protective microorganisms. 107 , 166”
From The battle for iron in enteric infections (2020) · cites this paper as [107]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Controlling the False Discovery Rate: A Practical and Powerful Approach to Multiple Testing
Benjamini, Y., & Hochberg, Y. (1995) · Journal of the Royal Statistical Society Series B: Statistical Methodology · doi:10.1111/j.2517-6161.1995.tb02031.x · Cited by 109,482
Moderated estimation of fold change and dispersion for RNA-seq data with DESeq2
Love, M. I., Huber, W., & Anders, S. (2014) · Genome Biology · doi:10.1186/s13059-014-0550-8 · Cited by 95,106
STAR: ultrafast universal RNA-seq aligner
Dobin, A., Davis, C. A., Schlesinger, F., Drenkow, J., Zaleski, C., Jha, S., Batut, P., Chaisson, M., & Gingeras, T. R. (2013) · Bioinformatics · doi:10.1093/bioinformatics/bts635 · Cited by 51,709
featureCounts: an efficient general purpose program for assigning sequence reads to genomic features
Liao, Y., Smyth, G. K., & Shi, W. (2014) · Bioinformatics · doi:10.1093/bioinformatics/btt656 · Cited by 27,219
A new method for non-parametric multivariate analysis of variance
Anderson, M. J. (2001) · Austral Ecology · doi:10.1111/j.1442-9993.2001.01070.pp.x · Cited by 13,828
Hepcidin Regulates Cellular Iron Efflux by Binding to Ferroportin and Inducing Its Internalization
Nemeth, E., Tuttle, M. S., Powelson, J., Vaughn, M. B., Donovan, A., Ward, D. M., Ganz, T., & Kaplan, J. (2004) · Science · doi:10.1126/science.1104742 · Cited by 4,803
Weiss, G., & Goodnough, L. T. (2005) · New England Journal of Medicine · doi:10.1056/nejmra041809 · Cited by 3,800
Nilsson, R. H., Larsson, K.-H., Taylor, A. F. S., Bengtsson‐Palme, J., Jeppesen, T. S., Schigel, D., Kennedy, P. G., Picard, K. T., Glöckner, F. O., Tedersoo, L., et al. (2018) · Nucleic Acids Research · doi:10.1093/nar/gky1022 · Cited by 3,660
Genetics and pathogenesis of inflammatory bowel disease
Khor, B., Gardet, A., & Xavier, R. J. (2011) · Nature · doi:10.1038/nature10209 · Cited by 2,733
Kaser, A., Zeissig, S., & Blumberg, R. S. (2010) · Annual Review of Immunology · doi:10.1146/annurev-immunol-030409-101225 · Cited by 1,806
Dysmetabolic Hyperferritinemia: All Iron Overload Is Not Hemochromatosis
Makker, J. S., Hanif, A., Bajantri, B., & Chilimuri, S. S. (2015) · Case Reports in Gastroenterology · doi:10.1159/000373883 · Cited by 1,353
A Red carpet for iron metabolism
Muckenthaler, M. U., Rivella, S., Hentze, M. W., & Galy, B. (2017) · Cell · doi:10.1016/j.cell.2016.12.034 · Cited by 1,319
The iron exporter ferroportin/Slc40a1 is essential for iron homeostasis
Donovan, A., Lima, C. A., Pinkus, J. L., Pinkus, G. S., Zon, L. I., Robine, S., & Andrews, N. C. (2005) · Cell Metabolism · doi:10.1016/j.cmet.2005.01.003 · Cited by 1,275
Innate Immunity Gone Awry: Linking Microbial Infections to Chronic Inflammation and Cancer
Karin, M., Lawrence, T., & Nizet, V. (2006) · Cell · doi:10.1016/j.cell.2006.02.016 · Cited by 938
FLEXBAR—Flexible Barcode and Adapter Processing for Next-Generation Sequencing Platforms
Dodt, M., Roehr, J. T., Ahmed-Begrich, R., & Dieterich, C. (2012) · Biology · doi:10.3390/biology1030895 · Cited by 721
Hepcidin and the iron-infection axis
Drakesmith, H., & Prentice, A. M. (2012) · Science · doi:10.1126/science.1224577 · Cited by 686 · cited 1×
“Iron sequestration is a key component of nutritional immunity (4, 18, 19), so we examined whether cDC-derived hepcidin alters the microbiota.”
BackgroundDrakesmith, H., Nemeth, E., & Ganz, T. (2015) · Cell Metabolism · doi:10.1016/j.cmet.2015.09.006 · Cited by 638
Hepcidin and disorders of iron metabolism
Ganz, T., & Nemeth, E. (2011) · Annual Review of Medicine · doi:10.1146/annurev-med-050109-142444 · Cited by 466
TLR4-dependent hepcidin expression by myeloid cells in response to bacterial pathogens
Peyssonnaux, C., Zinkernagel, A. S., Datta, V., Lauth, X., Johnson, R. S., & Nizet, V. (2006) · Blood · doi:10.1182/blood-2005-06-2259 · Cited by 379
Self-citationSasu, B. J., Cooke, K. S., Arvedson, T. L., Plewa, C., Ellison, A. R., Sheng, J., Winters, A., Juan, T., Li, H., Begley, C. G., et al. (2010) · Blood · doi:10.1182/blood-2009-09-245977 · Cited by 251
Self-citationHepcidin and Host Defense against Infectious Diseases
Michels, K., Nemeth, E., Ganz, T., & Mehrad, B. (2015) · PLOS Pathogens · doi:10.1371/journal.ppat.1004998 · Cited by 205
The Impact of Dietary Transition Metals on Host-Bacterial Interactions
Lopez, C. A., & Skaar, E. P. (2018) · Cell Host & Microbe · doi:10.1016/j.chom.2018.05.008 · Cited by 190
Bifidobacteria—Insight into clinical outcomes and mechanisms of its probiotic action
Sarkar, A., & Mandal, S. (2016) · Microbiological Research · doi:10.1016/j.micres.2016.07.001 · Cited by 190
An essential cell-autonomous role for hepcidin in cardiac iron homeostasis
Lakhal-Littleton, S., Wolna, M., Chung, Y. J., Christian, H. C., Heather, L. C., Brescia, M., Ball, V., Diaz, R., Santos, A., Biggs, D., et al. (2016) · eLife · doi:10.7554/elife.19804 · Cited by 184
Self-citationThe Role of Deferiprone in Iron Chelation
Hider, R. C., & Hoffbrand, A. V. (2018) · New England Journal of Medicine · doi:10.1056/nejmra1800219 · Cited by 153
Hepcidin agonists as therapeutic tools
Casu, C., Nemeth, E., & Rivella, S. (2018) · Blood · doi:10.1182/blood-2017-11-737411 · Cited by 136
Targeted disruption of hepcidin in the liver recapitulates the hemochromatotic phenotype
Zumerle, S., Mathieu, J. R. R., Delga, S., Heinis, M., Viatte, L., Vaulont, S., & Peyssonnaux, C. (2014) · Blood · doi:10.1182/blood-2014-01-550467 · Cited by 87
Self-citationRegulation of Hepcidin by Erythropoiesis: The Story So Far
Pasricha, S., McHugh, K., & Drakesmith, H. (2016) · Annual Review of Nutrition · doi:10.1146/annurev-nutr-071715-050731 · Cited by 84
High-throughput screening of small molecules identifies hepcidin antagonists
Fung, E., Sugianto, P., Hsu, J., Damoiseaux, R., Ganz, T., & Nemeth, E. (2013) · Molecular Pharmacology · doi:10.1124/mol.112.083428 · Cited by 78
Kayama, H., Kohyama, M., Okuzaki, D., Motooka, D., Barman, S., Okumura, R., Muneta, M., Hoshino, K., Sasaki, I., Ise, W., et al. (2018) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1808426115 · Cited by 55
Shanmugam, N. K. N., Trebicka, E., Fu, L.-L., Shi, H. N., & Cherayil, B. J. (2014) · The Journal of Immunology · doi:10.4049/jimmunol.1400278 · Cited by 49
Cited by
Sorted by citations
Mechanisms controlling cellular and systemic iron homeostasis
Galy, B., Conrad, M., & Muckenthaler, M. U. (2023) · Nature Reviews Molecular Cell Biology · doi:10.1038/s41580-023-00648-1 · Cited by 843
Sun, X., Zhang, Y., Li, J., Park, K. S., Han, K., Zhou, X., Xu, Y., Nam, J., Xu, J., Shi, X., et al. (2021) · Nature Nanotechnology · doi:10.1038/s41565-021-00962-9 · Cited by 808
Hepcidin-Ferroportin Interaction Controls Systemic Iron Homeostasis
Nemeth, E., & Ganz, T. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22126493 · Cited by 540
“In a mouse model of colitis, the hepcidin-ferroportin interaction in the intestine was shown to be important for mucosal healing [49].”
BackgroundMcCulloch, J. A., Davar, D., Rodrigues, R. R., Badger, J. H., Fang, J. R., Cole, A. M., Balaji, A. K., Vetizou, M., Prescott, S. M., Fernandes, M. R., et al. (2022) · Nature Medicine · doi:10.1038/s41591-022-01698-2 · Cited by 472
Hepcidin and Iron in Health and Disease
Nemeth, E., & Ganz, T. (2023) · Annual Review of Medicine · doi:10.1146/annurev-med-043021-032816 · Cited by 457
Metadata
- Authors
- Bessman, N. J., Mathieu, J. R. R., Renassia, C., Zhou, L., Fung, T. C., Fernandez, K. C., Austin, C., Moeller, J. B., Zumerle, S., Louis, S., Vaulont, S., Ajami, N. J., Sokol, H., Putzel, G. G., Arvedson, T., Sockolow, R. E., Lakhal-Littleton, S., Cloonan, S. M., Arora, M., Peyssonnaux, C., & Sonnenberg, G. F.
- Affiliations
- Cornell University (US)
- Centre National de la Recherche Scientifique (FR)
- Icahn School of Medicine at Mount Sinai (US)
- University of Southern Denmark (DK)
- The University of Texas MD Anderson Cancer Center (US)
- Inserm (FR)
- Amgen (United States) (US)
- Department of Physiology, Anatomy and Genetics, University of Oxford, Oxford OX1 3PT, UK.
- Trinity College Dublin (IE)
- Corresponding author
- Mathieu, Jacques R. R.
- Renassia, Cyril
- Peyssonnaux, Carole
- Sonnenberg, Gregory F.
- ORCID
- Bessman, Nicholas J.
- Mathieu, Jacques R. R.
- Renassia, Cyril
- Zhou, Lei
- Fung, Thomas C.
- Fernandez, Keith C.
- Austin, Christine
- Moeller, Jesper B.
- Zumerle, Sara
- Vaulont, Sophie
- Ajami, Nadim J.
- Sokol, Harry
- Putzel, Gregory G.
- Arvedson, Tara
- Sockolow, Robbyn E.
- Lakhal-Littleton, Samira
- Cloonan, Suzanne M.
- Arora, Manish
- Peyssonnaux, Carole
- Sonnenberg, Gregory F.
- Venue
- Science
- Published
- 2020-04-10
- Volume
- 368
- Issue
- 6487
- Pages
- 186-189
- ISSN
- 0036-8075 (ISSN-L)
- 1095-9203
- PMC
- PMC7724573
- OpenAlex
- W3015399161
- Cited by
- 145
- References
- 32
- Citations by year
- 2026: 14 · 2025: 23 · 2024: 17 · 2023: 31 · 2022: 16 · 2021: 21 · 2020: 22
- FWCI
- 14.20
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Licence
- other-oa
- Locations
- Science (publishedVersion)
- University of Southern Denmark Research Portal (University of Southern Denmark) (publishedVersion, other-oa)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Trinity's Access to Research Output (TARA) (Trinity College Dublin) (submittedVersion)
- Arrow@dit (Dublin Institute of Technology) (submittedVersion)
- HAL (submittedVersion)
- Padua Research Archive (University of Padova) (submittedVersion, other-oa)
- Funders
- NIH Office of the Director (OD012116)
- National Institute of Allergy and Infectious Diseases (AI124517, AI123368, U01AI095608, AI145989, AI143482)
- European Research Council (261296)
- Fondation pour la Recherche Médicale (DEQ20160334903)
- National Institute of Environmental Health Sciences (U2CES030859, P30ES023515, P30 ES023515)
- National Institute of Diabetes and Digestive and Kidney Diseases (DK110262)
- Burroughs Wellcome Fund
- Crohn"s and Colitis Foundation of America
- American Asthma Foundation
- Searle Scholars Program
- Eunice Kennedy Shriver National Institute of Child Health and Human Development (R00HD087523)
- French National Research Agency (ANR-11-IDEX-0005-02)
- Laboratory of Excellence GR-Ex (ANR-11-LABX-0051)
- Roberts Institute for Research in IBD
- Crohn’s and Colitis Foundation (608975)
- Topics
- Health Sciences › Medicine › Hematology › Iron Metabolism and Disorders
- Health Sciences › Medicine › Gastroenterology › Inflammatory Bowel Disease
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Gut microbiota and health
- Keywords
- hepcidin, myeloid dendritic cells, intestinal mucosal healing, iron sequestration, gut microbiota, ferroportin, nutritional immunity, iron homeostasis, intestinal inflammation
- MeSH terms
- Gastrointestinal Microbiome, Fecal Microbiota Transplantation, Ferroportin, Animals, Dendritic Cells, Homeostasis, Intestinal Diseases, Intestinal Mucosa, Iron, Mice, Mutant Strains, Phagocytes, Gene Deletion, Cation Transport Proteins, Mice, Hepcidins
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review